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MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type

Neuroradiology, 1997-05, Vol.39 (5), p.371-377

1997

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Hippocampal lesions in the neuronal ceroid lipofuscinoses

European journal of paediatric neurology, 2001, Vol.5 Suppl A, p.209-211

2001

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Congenital ovine neuronal ceroid lipofuscinosis--a cathepsin D deficiency with increased levels of the inactive enzyme

European journal of paediatric neurology, 2001, Vol.5 Suppl A, p.43-45

2001

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Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)

Clinical genetics, 1991-04, Vol.39 (4), p.287-293

1991

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Familial Creutzfeldt-Jakob Disease in Finland: Epidemiological, Clinical, Pathological and Molecular Genetic Studies

European journal of epidemiology, 1991-09, Vol.7 (5), p.494-500

1991

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An autosomal locus predisposing to deletions of mitochondrial DNA

Nature genetics, 1995-02, Vol.9 (2), p.146-151

1995

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Isolation of human immunodeficiency virus (HIV) at autopsy one to six days postmortem

American journal of clinical pathology, 1990-10, Vol.94 (4), p.422-425

1990

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E. A. Homén ja hepatolentikulaarisen degeneraation keksiminen

Hippokrates (Helsinki, Finland), 1992, Vol.9, p.99

Haltia, M

1992

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Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis

FEBS letters, 1993-09, Vol.330 (1), p.8-12

1993

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ORIGINAL ARTICLE: Cutis laxa in hereditary gelsolin amyloidosis

British journal of dermatology (1951), 2005-02, Vol.152 (2), p.250-257

2005

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Genetic association of α2-macroglobulin with Alzheimer's disease in a Finnish elderly population

Annals of neurology, 1999-09, Vol.46 (3), p.382-390

1999

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Microangiopathy with encephalopathy, hearing loss and retinal arteriolar occlusions: Two new cases

Journal of the neurological sciences, 1988-09, Vol.86 (2), p.239-250

1988

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Amphoterin includes a sequence motif which is homologous to the Alzheimer's beta-amyloid peptide (Abeta), forms amyloid fibrils in vitro, and binds avidly to Abeta

Biochemistry (Easton), 2001-08, Vol.40 (34), p.10032-10037

2001

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Amyloid β protein (Aβ) deposition in chromosome 14-linked Alzheimer's disease: Predominance of Aβ42(43)

Annals of neurology, 1996-08, Vol.40 (2), p.149-156

1996

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Chronology of Lake El'gygytgyn sediments

Climate of the past, 2013-11, Vol.9 (6), p.2413

2013

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Hormone treatment of meningiomas: lack of response to medroxyprogesterone acetate (MPA): a pilot study of five cases

Acta neurochirurgica, 1986-03, Vol.80 (1-2), p.35-41

1986

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Synthetic Peptides Corresponding to Different Mutated Regions of the Amyloid Gene in Familial Creutzfeldt-Jakob Disease Show Enhanced in vitro Formation of Morphologically Different Amyloid Fibrils

Proceedings of the National Academy of Sciences - PNAS, 1993-05, Vol.90 (10), p.4451-4454

1993

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High-mannose dolichol-linked oligosaccharides in infantile ceroid-lipofuscinosis

Biochemical Society transactions, 1989-12, Vol.17 (6), p.1032-1033

1989

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Postnatal development of spinal anterior horn neurones in normal and undernourished rats. A quantitative cytochemical study

Acta physiologica Scandinavica. Supplementum, 1970, Vol.352, p.1

Haltia, M

1970

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Introduction

Neuropediatrics, 1997-02, Vol.28 (1), p.3-3

1997

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"Amaurotic idiocy"

Duodecim (Helsinki, Finland : 1961), 1975, Vol.91 (6), p.312

Haltia, M

1975

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Diagnosis of intracranial haemangiopericytomas with angiography and CT scanning

Neuroradiology, 1985, Vol.27 (1), p.38-43

1985

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Suomen neurologian alkuvaiheita

Hippokrates (Helsinki, Finland), 1986, Vol.3, p.150

1986

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The structure of the presenilin 1 ( S182 ) gene and identification of six novel mutations in early onset AD families

MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type

Hippocampal lesions in the neuronal ceroid lipofuscinoses

Congenital ovine neuronal ceroid lipofuscinosis--a cathepsin D deficiency with increased levels of the inactive enzyme

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)

Familial Creutzfeldt-Jakob Disease in Finland: Epidemiological, Clinical, Pathological and Molecular Genetic Studies

An autosomal locus predisposing to deletions of mitochondrial DNA

Isolation of human immunodeficiency virus (HIV) at autopsy one to six days postmortem

Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-β concentrations

E. A. Homén ja hepatolentikulaarisen degeneraation keksiminen

Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis

ORIGINAL ARTICLE: Cutis laxa in hereditary gelsolin amyloidosis

Genetic association of α2-macroglobulin with Alzheimer's disease in a Finnish elderly population

Microangiopathy with encephalopathy, hearing loss and retinal arteriolar occlusions: Two new cases

Amphoterin includes a sequence motif which is homologous to the Alzheimer's beta-amyloid peptide (Abeta), forms amyloid fibrils in vitro, and binds avidly to Abeta

Amyloid β protein (Aβ) deposition in chromosome 14-linked Alzheimer's disease: Predominance of Aβ42(43)

Chronology of Lake El'gygytgyn sediments

Hormone treatment of meningiomas: lack of response to medroxyprogesterone acetate (MPA): a pilot study of five cases

Synthetic Peptides Corresponding to Different Mutated Regions of the Amyloid Gene in Familial Creutzfeldt-Jakob Disease Show Enhanced in vitro Formation of Morphologically Different Amyloid Fibrils

High-mannose dolichol-linked oligosaccharides in infantile ceroid-lipofuscinosis

Postnatal development of spinal anterior horn neurones in normal and undernourished rats. A quantitative cytochemical study

Introduction

"Amaurotic idiocy"

Diagnosis of intracranial haemangiopericytomas with angiography and CT scanning

Suomen neurologian alkuvaiheita

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